Methylamine → N-Methyl-o-toluenesulfonamide
反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8](Cl)(=[O:10])=[O:9].[CH3:12][NH2:13]>C(Cl)Cl>[CH3:12][NH:13][S:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[CH3:1])(=[O:10])=[O:9]参加物
4
実験手順
To a solution of 2-methylbenzenesulfonyl chloride (37.4 g, 0.196 mol) in methylene chloride (300 ml) at -5° to 0° under nitrogen was added liquid methylamine (27.5 ml, 0.588 mol) at a rate to maintain an internal temperature less than 10°. The reaction mixture was stirred at 0° for 1/2 hour and then allowed to warm to room temperature. After 11/4 hours, filtration and concentration of the filtrate gave an oil which solidified upon cooling. Washing the solid with n-butyl chloride gave N,2-dimethylbenzenesulfonamide as a light yellow powder (28.4 g, 78%), mp. 62°-64°.
後処理
- temperatureto maintain an internal temperature less than 10°
- filtrationAfter 11/4 hours, filtration and concentration of the filtrate
- customgave an oil which
- temperatureupon cooling
- washWashing the solid with n-butyl chloride
出典と根拠
- ORDレコード
- ord-7c10f760bd43447a864f33b5e4e39c09
- 出典データセット
- uspto-grants-1984_06
- 特許番号
- US04454135
反応ノート
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